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      Clinical interventions that influence vaginal birth after cesarean delivery rates: Systematic Review & Meta-Analysis

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          Abstract

          Background

          To systematically review the literature on clinical interventions that influence vaginal birth after cesarean (VBAC) rates.

          Methods

          We searched Ovid Medline, Ovid Embase, Wiley Cochrane Library, CINAHL via EBSCOhost; and Ovid PsycINFO. Additional studies were identified by searching for clinical trial records, conference proceedings and dissertations. Limits were applied for language (English and French) and year of publication (1985 to present). Two reviewers independently screened comparative studies (randomized or non-randomized controlled trials, and observational designs) according to a priori eligibility criteria: women with prior cesarean sections; any clinical intervention or exposure intended to increase the VBAC rate; any comparator; and, outcomes reporting VBAC, uterine rupture and uterine dehiscence rates. One reviewer extracted data and a second reviewer verified for accuracy. Meta-analysis was conducted using Mantel-Haenszel (random effects model) relative risks (VBAC rate) and risk differences (uterine rupture and dehiscence). Two reviewers independently conducted methodological quality assessments using the Mixed Methods Appraisal Tool (MMAT).

          Results

          Twenty-nine studies (six trials and 23 cohorts) examined different clinical interventions affecting rates of vaginal deliveries among women with a prior cesarean delivery (CD). Methodological quality was good overall for the trials; however, concerns among the cohort studies regarding selection bias, comparability of groups and outcome measurement resulted in higher risk of bias. Interventions for labor induction, with or without cervical ripening, included pharmacologic (oxytocin, prostaglandins, misoprostol, mifepristone, epidural analgesia), non-pharmacologic (membrane sweep, amniotomy, balloon devices), and combined (pharmacologic and non-pharmacologic). Single studies with small sample sizes and event rates contributed to most comparisons, with no clear differences between groups on rates of VBAC, uterine rupture and uterine dehiscence.

          Conclusions

          This systematic review evaluated clinical interventions directed at increasing the rate of vaginal delivery among women with a prior CD and found low to very low certainty in the body of evidence for cervical ripening and/or labor induction techniques. There is insufficient high-quality evidence to inform optimal clinical interventions among women attempting a trial of labor after a prior CD.

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          Most cited references60

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          ACOG Practice Bulletin No. 205: Vaginal Birth After Cesarean Delivery.

          (2019)
          Trial of labor after cesarean delivery (TOLAC) refers to a planned attempt to deliver vaginally by a woman who has had a previous cesarean delivery, regardless of the outcome. This method provides women who desire a vaginal delivery the possibility of achieving that goal-a vaginal birth after cesarean delivery (VBAC). In addition to fulfilling a patient's preference for vaginal delivery, at an individual level, VBAC is associated with decreased maternal morbidity and a decreased risk of complications in future pregnancies as well as a decrease in the overall cesarean delivery rate at the population level (). However, although TOLAC is appropriate for many women, several factors increase the likelihood of a failed trial of labor, which in turn is associated with increased maternal and perinatal morbidity when compared with a successful trial of labor (ie, VBAC) and elective repeat cesarean delivery (). Therefore, assessing the likelihood of VBAC as well as the individual risks is important when determining who is an appropriate candidate for TOLAC. Thus, the purpose of this document is to review the risks and benefits of TOLAC in various clinical situations and to provide practical guidelines for counseling and management of patients who will attempt to give birth vaginally after a previous cesarean delivery.
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            The MFMU Cesarean Registry: factors affecting the success of trial of labor after previous cesarean delivery.

            The purpose of this study was to determine which factors influence the likelihood of successful trial of labor (TOL) after 1 previous cesarean delivery (CD). We performed a multicenter 4-year prospective observational study (1999-2002) of all women with previous CD undergoing TOL. Women with term singleton pregnancies with 1 previous low transverse CD or unknown incision were included for analysis. Fourteen thousand five hundred twenty-nine women underwent TOL, with 10,690 (73.6%) achieving successful VBAC. Women with previous vaginal birth had an 86.6% success rate compared with 60.9% in women without such a history (odds ratio [OR] 4.2; 95% CI 3.8-4.5; P or = 30) was lower (68.4%) than in nonobese women (79.6%) (P or = 30 significantly lowers success rates.
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              Induction of labour for improving birth outcomes for women at or beyond term

              Beyond term, the risks of stillbirth or neonatal death increase. It is unclear whether a policy of labour induction can reduce these risks. This Cochrane review is an update of a review that was originally published in 2006 and subsequently updated in 2012 To assess the effects of a policy of labour induction at or beyond term compared with a policy of awaiting spontaneous labour or until an indication for birth induction of labour is identified) on pregnancy outcomes for infant and mother. We searched Cochrane Pregnancy and Childbirth’s Trials Register, ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform ( ICTRP ) (9 October 2017), and reference lists of retrieved studies. Randomised controlled trials (RCTs) conducted in pregnant women at or beyond term, comparing a policy of labour induction with a policy of awaiting spontaneous onset of labour (expectant management). We also included trials published in abstract form only. Cluster‐RCTs, quasi‐RCTs and trials using a cross‐over design are not eligible for inclusion in this review. We included pregnant women at or beyond term. Since a risk factor at this stage of pregnancy would normally require an intervention, only trials including women at low risk for complications were eligible. We accepted the trialists' definition of 'low risk'. The trials of induction of labour in women with prelabour rupture of membranes at or beyond term were not considered in this review but are considered in a separate Cochrane review. Two reviewers independently assessed trials for inclusion, assessed risk of bias and extracted data. Data were checked for accuracy. We assessed the quality of evidence using the GRADE approach. In this updated review, we included 30 RCTs (reporting on 12,479 women). The trials took place in Norway, China, Thailand, the USA, Austria, Turkey, Canada, UK, India, Tunisia, Finland, Spain, Sweden and the Netherlands. They were generally at a moderate risk of bias. Compared with a policy of expectant management, a policy of labour induction was associated with fewer (all‐cause) perinatal deaths (risk ratio (RR) 0.33, 95% confidence interval (CI) 0.14 to 0.78; 20 trials, 9960 infants; moderate‐quality evidence). There were two perinatal deaths in the labour induction policy group compared with 16 perinatal deaths in the expectant management group. The number needed to treat to for an additional beneficial outcome (NNTB) with induction of labour in order to prevent one perinatal death was 426 (95% CI 338 to 1337). There were fewer stillbirths in the induction group (RR 0.33, 95% CI 0.11 to 0.96; 20 trials, 9960 infants; moderate‐quality evidence); there was one stillbirth in the induction policy arm and 10 in the expectant management group. For women in the policy of induction arms of trials, there were fewer caesarean sections compared with expectant management (RR 0.92, 95% CI 0.85 to 0.99; 27 trials, 11,738 women; moderate‐quality evidence); and a corresponding marginal increase in operative vaginal births with induction (RR 1.07, 95% CI 0.99 to 1.16; 18 trials, 9281 women; moderate‐quality evidence). There was no evidence of a difference between groups for perineal trauma (RR 1.09, 95% CI 0.65 to 1.83; 4 trials; 3028 women; low‐quality evidence), postpartum haemorrhage (RR 1.09 95% CI 0.92 to 1.30, 5 trials; 3315 women; low‐quality evidence), or length of maternal hospital stay (average mean difference (MD) ‐0.34 days, 95% CI ‐1.00 to 0.33; 5 trials; 1146 women; Tau² = 0.49; I² 95%; very low‐quality evidence). Rates of neonatal intensive care unit (NICU) admission were lower (RR 0.88, 95% CI 0.77 to 1.01; 13 trials, 8531 infants; moderate‐quality evidence) and fewer babies had Apgar scores less than seven at five minutes in the induction groups compared with expectant management (RR 0.70, 95% CI 0.50 to 0.98; 16 trials, 9047 infants; moderate‐quality evidence). There was no evidence of a difference for neonatal trauma (RR 1.18, 95% CI 0.68 to 2.05; 3 trials, 4255 infants; low‐quality evidence), for induction compared with expectant management. Neonatal encephalopathy, neurodevelopment at childhood follow‐up, breastfeeding at discharge and postnatal depression were not reported by any trials. In subgroup analyses, no clear differences between timing of induction ( 287 days) gestation for the intervention arm. A policy of labour induction at or beyond term compared with expectant management is associated with fewer perinatal deaths and fewer caesarean sections; but more operative vaginal births. NICU admissions were lower and fewer babies had low Apgar scores with induction. No important differences were seen for most of the other maternal and infant outcomes. Most of the important outcomes assessed using GRADE had a rating of moderate or low‐quality evidence ‐ with downgrading decisions generally due to study limitations such as lack of blinding (a condition inherent in comparisons between a policy of acting and of waiting), or imprecise effect estimates. One outcome (length of maternal stay) was downgraded further to very low‐quality evidence due to inconsistency. Although the absolute risk of perinatal death is small, it may be helpful to offer women appropriate counselling to help choose between scheduled induction for a post‐term pregnancy or monitoring without (or later) induction). The optimal timing of offering induction of labour to women at or beyond term warrants further investigation, as does further exploration of risk profiles of women and their values and preferences. Individual participant meta‐analysis is likely to help elucidate the role of factors, such as parity, in influencing outcomes of induction compared with expectant management. Induction of labour in women with normal pregnancies at or beyond term What is the issue? A normal pregnancy lasts about 40 weeks from the start of the woman's last menstrual period, but anything from 37 to 42 weeks is considered as being at term (within the normal range). If a pregnancy goes too long, a woman and her clinician may wish to intervene to bring the birth on, for example, by induction. Why is this important? Births after 42 weeks' gestation may slightly increase risks for babies, including a greater risk of death (before or shortly after birth). However induction of labour may also have risks for mothers and their babies, especially if women are not ready to labour. No tests can predict if babies would be better to stay inside their mother or if labour should be induced to make the birth happen sooner. Many hospitals therefore have policies for how long pregnancies should continue. This update (originally published in 2006 and subsequently updated in 2012) looks to see if inducing labour at a set time at or beyond term, could reduce risks for the babies. What evidence did we find? We searched for evidence up 9 October 2017 and identified 30 trials with over 12,000 women. The trials took place in Norway, China, Thailand, the USA, Austria, Turkey, Canada, UK, India, Tunisia, Finland, Spain, Sweden and the Netherlands. The evidence was mostly of moderate quality. The trials compared a policy to induce labour at or later than term (usually after 41 completed weeks of gestation (> 287 days)) with waiting for labour to start and/or waiting for a period before inducing labour. We found that there were fewer deaths of babies in hospitals with a policy to induce when a pregnancy was continuing beyond term (moderate‐quality evidence). Fewer caesarean births were required with induction compared with waiting, but more assisted vaginal births were required with induction. There were fewer admissions to the intensive care nursery and fewer low Apgar scores at five minutes after birth (a simple test to test babies' health) in the induction groups compared with waiting (moderate‐quality evidence). We found that there were no clear differences between a policy to induce at or later than term or waiting in the risks of mothers having trauma to their perineum or bleeding after birth (both low‐quality evidence), in the length of their hospital stay (very‐low quality evidence), or in their babies having trauma (low‐quality evidence), None of the trials provided information on breastfeeding at discharge from hospital, postnatal depression, or whether the babies had encephalopathy (early abnormal neurological function), or child development. What does this mean? A policy of labour induction compared with expectant management is associated with fewer deaths of babies and fewer caesarean sections; but more assisted vaginal births. Although the chances of babies dying are small, it may help to offer women appropriate counselling to make an informed choice between induction of labour for pregnancies at, or later than, term ‐ or waiting for labour to start and/or waiting before inducing labour. The best time to offer induction of labour to women at or beyond term is not yet clear and warrants further investigation. The risk profiles of women as well as their values and preferences could also be considered.
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                Author and article information

                Contributors
                awingert@ualberta.ca
                hartling@ualberta.ca
                sebastianski@ualberta.ca
                cydney1@ualberta.ca
                feathers@ualberta.ca
                bv1@ualberta.ca
                doug.wilson@ahs.ca
                Journal
                BMC Pregnancy Childbirth
                BMC Pregnancy Childbirth
                BMC Pregnancy and Childbirth
                BioMed Central (London )
                1471-2393
                30 December 2019
                30 December 2019
                2019
                : 19
                : 529
                Affiliations
                [1 ]GRID grid.17089.37, Department of Pediatrics, Alberta Research Centre for Health Evidence, , University of Alberta, ; Edmonton, Alberta Canada
                [2 ]GRID grid.17089.37, Alberta Strategy for Patient-Oriented Research (SPOR) SUPPORT Unit Knowledge Translation Platform, , University of Alberta, ; Edmonton, Alberta Canada
                [3 ]ISNI 0000 0004 1936 7697, GRID grid.22072.35, Department of Obstetrics and Gynecology, Cumming School of Medicine, , University of Calgary, ; 1403 – 29 Street NW, Calgary, AB T2N 2T9 Canada
                Article
                2689
                10.1186/s12884-019-2689-5
                6937863
                31888540
                621f3c4d-a6fa-4d28-adb6-3d6fc2de480c
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 30 May 2019
                : 19 December 2019
                Funding
                Funded by: Maternal, Newborn, Child and Youth Strategic Clinical Network (MNCY SCN) of Alberta Health Services (AHS)
                Funded by: Alberta Strategy for Patient-Oriented Research (SPOR) SUPPORT Unit Knowledge Translation Platform
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Obstetrics & Gynecology
                vaginal birth after cesarean,trial of labor after cesarean,systematic review,meta-analysis

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